Up And Up Daytime Multi Symptom Severe Cold Nighttime Severe Cold And Cough Kit
NDC Package 11673-877-55

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is approaching its end of marketing date. An upcoming end of marketing date means the product has been delisted but will remain in the NDC database until the end of marketing date is reached. In most cases, the FDA advises firms to use the expiration date of the last lot produced as the end marketing date, reflecting the possibility that the product may still be available even after manufacturing has stopped.

Up And Up Daytime Multi Symptom Severe Cold Nighttime Severe Cold And Cough (acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride, diphenhydramine hydrochloride) kits is •do not use more than directed (see overdose warning)•take every 4 hours, while symptoms persist. This formulation utilizes a kit delivery system. Marketed by Target Corporation, this product is identified by NDC 11673-877 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
11673-877-55
Package Description
1 KIT in 1 CARTON * 1 POWDER, FOR SOLUTION in 1 PACKET (82442-122-00) * 1 POWDER, FOR SOLUTION in 1 PACKET (82442-964-00)
Product Code
11673-877
11-Digit Billing Format
11673087755
RxNorm Crosswalk
  • RxCUI: 1189316 - acetaminophen 500 MG / dextromethorphan HBr 20 MG / phenylephrine HCl 10 MG Granules for Oral Solution
  • RxCUI: 1189316 - acetaminophen 500 MG / dextromethorphan hydrobromide 20 MG / phenylephrine hydrochloride 10 MG Granules for Oral Solution
  • RxCUI: 1189316 - acetaminophen 500 MG / dextromethorphan HBr 20 MG / phenylephrine HCl 10 MG Packet for Oral Solution
  • RxCUI: 1189316 - acetaminophen 500 MG / dextromethorphan hydrobromide 20 MG / phenylephrine hydrochloride 10 MG Powder for Oral Solution
  • RxCUI: 1189316 - APAP 500 MG / Dextromethorphan Hydrobromide 20 MG / Phenylephrine Hydrochloride 10 MG Granules for Oral Solution

Clinical Specifications

Proprietary Name
Up And Up Daytime Multi Symptom Severe Cold Nighttime Severe Cold And Cough
Non-Proprietary Name
Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, Diphenhydramine Hydrochloride
Dosage Form
Kit - A packaged collection of related material.
Usage Information
•do not use more than directed (see overdose warning)•take every 4 hours, while symptoms persist. Do not take more than 6 packets in 24 hours unless directed by a doctor.AgeDoseadults and children 12 years of age and overone packetchildren under 12 years of agedo not use•dissolve contents of one packet into 8 oz. hot water: sip while hot. Consume entire drink within 10-15 minutes.•if using a microwave, add contents of one packet to 8 oz. of cool water: stir briskly before and after heating. Do not overheat. •do not use more than directed (see overdose warning)•take every 4 hours, while symptoms persist. Do not take more than 5 packets in 24 hours unless directed by a doctor.AgeDoseadults and children 12 years of age and overone packetchildren under 12 years of agedo not use•dissolve contents of one packet into 8 oz. hot water: sip while hot. Consume entire drink within 10-15 minutes.•if using a microwave, add contents of one packet to 8 oz. of cool water: stir briskly before and after heating. Do not overheat.

Regulatory & Marketing

Labeler Name
Target Corporation
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-16-2021
End Marketing Date
08-01-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 11673-877-55 identifies a specific commercial package of 1 kit in 1 carton * 1 powder, for solution in 1 packet (82442-122-00) * 1 powder, for solution in 1 packet (82442-964-00) of Up And Up Daytime Multi Symptom Severe Cold Nighttime Severe Cold And Cough, a human over the counter drug labeled by Target Corporation. This kit is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Target Corporation on July 16, 2021.

How is this Target Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 11673087755. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
11673-877-55
11-Digit CMS (5-4-2)
11673-0877-55

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.